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Lifestyle Intervention for Pakistani Women in Oslo (InnvaDiab)

2014年6月24日 更新者:Gerd Holmboe-Ottesen、University of Oslo

Evaluation of a Lifestyle Intervention to Prevent Type 2 Diabetes/Metabolic Syndrome Among Pakistani Immigrants - Focusing on Changes in Diet and Physical Activity

Immigrants from South Asia in Norway have a high prevalence of type 2 diabetes and conditions related to the metabolic syndrome. It has been documented that these conditions may be prevented by changes in lifestyle. No previous intervention studies on immigrants with focus on diet and physical activity have been carried out in Norway. This project concerns a randomized controlled trial with intervention to change diet and physical activity in 200 high risk female Pakistani immigrants living in Oslo. The intervention will be evaluated both in terms of outcome and process.

調査の概要

詳細な説明

Objectives:

  1. To evaluate the health effects of systematic dietary education and counselling and physical training in a group of Pakistani women with high risk of type 2 diabetes.
  2. To evaluate the intervention process in order to identify the most effective methods of intervention in regard to diet and physical activity for immigrant women of Pakistani origin.

Background: Immigrants from South Asia have a high prevalence of type 2 diabetes, which may be prevented by intensive on physical activity and diet. This application concerns intervention with diet and physical activity in female (ongoing study) and male (extended study) Pakistani immigrants living in Oslo to reduce their risk for these diseases.

Intervention design: The subjects will be 200 women randomized into an intervention group and a control group (100 in each). The women are being recruited from a township in Oslo with a high proportion of immigrants by using a network approach. Inclusion criteria is based on a risk score developed by Ramachandran et al for Asian Indians, entailing age, Body Mass Index, waist circumference, family history of diabetes and sedentary physical activity.

The intervention will include a combination of individual counselling and group sessions. The intervention group will be divided into subgroups of 10-12 subjects. Each subgroup will have 10 group sessions on diet/lifestyle in the 6 months the intervention period lasts, and will additionally have the possibility to join a cultural adapted exercise program of low intensity twice a week. This includes indoor activities (exercise with music) and outdoor activities (walking groups).

Evaluation: The main end point of the intervention will be the fasting and 2-h plasma glucose value after an oral glucose tolerance test (OGTT). This will be measured at baseline and after 6 months of intervention.

Secondary end-points will be Serum lipid profile (e.g. triglycerides, High-Density Lipoprotein-cholesterol) ; HbA1c ; C-peptide ; serum insulin; serum albumin; body weight; waist and hip circumference; maximum heart rate on treadmill test; self-reported level of intensity, duration and frequency of physical activity; self-reported level of "Stages of change" in regard to motivation and behavioural change; self- reported subjective health complaints; self-reported coping strategies; self-reported sleeping habits.

Dietary information will be collected by 2 x 48 hours dietary recalls. The intake of energy and nutrients will be calculated from the recalls, as well as the intake of food groups.The diet will also be evaluated by a culturally adapted food frequency questionnaire including 20 food groups (with portion sizes). In addition, the use of cooking oils will be registered by questions about the type and quantity oil used per time unit in the household. Additionally, information on knowledge and perceptions on diet and health before and after the intervention will be registered.

Physical activity will be registered using an advanced continuous body monitor, SenseWear Armband yielding information on total energy expenditure, level of intensity, duration and frequency of physical activity, duration of lying down, duration of sleeping, and sleeping quality.

The completion of the questionnaires will take the form of an interview by Urdu speaking staff.

研究の種類

介入

入学 (実際)

198

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Holmlia, Oslo
      • Oslo、Holmlia, Oslo、ノルウェー、1255
        • Primary Health Care Health Center

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

25年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

はい

受講資格のある性別

女性

説明

Inclusion Criteria:

  • Risk score developed by Ramachandran et al for Asian Indians:

    • BMI, waist circumference, family history of diabetes and sedentary physical activity

Exclusion Criteria:

  • Type 1 diabetes.
  • Positive auto antibodies.
  • Diagnosis of type 2 diabetes more than 6 months.
  • Medication for type 2 diabetes.
  • Pregnancy at intervention start.
  • Suffering from heart attack or stroke the last 3 months.
  • Already participating in organised physical exercise.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:防止
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Intervention
The intervention group was divided into nine subgroups of ten to twelve women who were offered six educational sessions, each lasting 2 h, during a 7 +- 1-month period. The main focus was on the physiological importance of blood glucose and its regulation by diet and physical activity, and on knowledge about the Pakistani lifestyle in Pakistan and Norway
The intervention will include a combination of individual counselling group sessions. The intervention groups will be divided into subgroups of 10-12 subjects. Each group will have 10 group sessions on diet/lifestyle in the 6 months the intervention period lasts, and will additionally have the possibility to join a culturally adapted exercise program of low intensity twice a week.
介入なし:Control
One lesson recieved after post-test

この研究は何を測定していますか?

主要な結果の測定

結果測定
時間枠
The Fasting Plasma Glucose Value, Baseline
時間枠:baseline
baseline
Plasma Glucose 2 h After Oral Glucose Tolerance Test, Baseline
時間枠:baseline
baseline
The Fasting Plasma Glucose, Post-test
時間枠:post-test
post-test
Plasma Glucose, 2-h, Post-test
時間枠:post-test
post-test

二次結果の測定

結果測定
時間枠
HbA1c, Baseline
時間枠:baseline
baseline
C-peptide, 0-h, Baseline
時間枠:baseline
baseline
C-peptid, 2-h, Baseline
時間枠:baseline
baseline
Insulin, 0-h, Baseline
時間枠:baseline
baseline
Insulin, 2-h, Baseline
時間枠:baseline
baseline
High-Density Lipoprotein Cholesterol, Baseline
時間枠:baseline
baseline
Triglycerides, Baseline
時間枠:baseline
baseline
Systolic Blood Pressure, Baseline
時間枠:baseline
baseline
Diastolic Blood Pressure, Baseline
時間枠:baseline
baseline
Waist Circumference, Baseline
時間枠:baseline
baseline
Body Mass Index, Baseline
時間枠:baseline
baseline
Intake of Vegetables, Fruit and Fruit Juice, Baseline
時間枠:baseline
baseline
Intake of Soft Drinks With Added Sugar, Baseline
時間枠:baseline
baseline
Intake of Red Meat, Baseline
時間枠:baseline
baseline
Intake of Poultry, Baseline
時間枠:baseline
baseline
Intake of Fish, Baseline
時間枠:baseline
baseline
HbA1C, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
C-peptid, 0-h, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
C-peptid, 2-h, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
Insulin, 0-h, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
Insulin, 2-h, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
High-Density Lipoprotein Cholesterol, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
Triglycerides, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
Systolic Blood Pressure, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
Diastolic Blood Pressure, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
Waist Circumference
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
Body Mass Index, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
Intake of Vegetables, Fruit and Fruit Juice, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
Intake of Soft Drinks With Added Sugar, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
Intake of Red Meat, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
Intake of Poultry, Post-test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions
Intake of Fish, Post Test
時間枠:post-test, after completion of all six group sessions
post-test, after completion of all six group sessions

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Gerd Holmboe-Ottesen, Dr. Philos.、University of Oslo

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2006年4月1日

一次修了 (実際)

2008年9月1日

研究の完了 (実際)

2008年9月1日

試験登録日

最初に提出

2007年1月19日

QC基準を満たした最初の提出物

2007年1月19日

最初の投稿 (見積もり)

2007年1月22日

学習記録の更新

投稿された最後の更新 (見積もり)

2014年7月21日

QC基準を満たした最後の更新が送信されました

2014年6月24日

最終確認日

2014年4月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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